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Clinical Evaluation of Medical Device Software and Software as a Medical Device

Length
1 day
Price
649 GBP 549 GBP
Next course start
22 January, 2025 (+3 start dates)
Course delivery
Virtual Classroom
Length
1 day
Price
649 GBP 549 GBP
Next course start
22 January, 2025 (+3 start dates)
Course delivery
Virtual Classroom
Visit this course's homepage on the provider's site to learn more or book!

Clinical Evaluation of Medical Device Software and Software as a Medical Device

Whether developing new medical software for more precise diagnosis and targeted treatment or a healthcare app for individuals concerned about their health, manufacturers are tasked to appreciably prove to authorities the safety, quality, and effectiveness of their products. The evaluation of clinical safety and performance, as well as the overall benefit‑risk profile of the product, through a critical assessment of relevant data, is one of the key requirements for the manufacturers of a medical device software and a focus area for regulators.

This course will provide a clear understanding of the the clinical evaluation requirements and their practical application for software products, including AI/ML-based devices. It will also provide advice on how to determine the type and amount of data needed to sufficiently support the intended medical purpose and (individual) clinical claims, with many practical examples and analysis of differences between EU MDR and FDA approach.

Upcoming start dates

Choose between 3 start dates

22 January, 2025

  • Virtual Classroom
  • Online
  • English

13 May, 2025

  • Virtual Classroom
  • Online
  • English

1 October, 2025

  • Virtual Classroom
  • Online
  • English

Suitability - Who should attend?

Benefits of attending

  • Gain an in-depth understanding of the requirements for clinical evaluation and how to apply them to different types of medical device software, including AI/ML-based devices
  • Understand how to establish measurable endpoints for clinical claims 
  • Find out how to define and generate sufficient clinical and/or performance data to meet the safety and performance requirements of your software device
  • Witness the role of human factors and risks
  • Learn how to retrieve and use literature data effectively
  • Identify residual clinical risks and determine whether post-market clinical follow-up is required
  • Provide robust documentation in support of the clinical safety and performance of your device
  • Hear about frequent pitfalls of clinical regulatory submissions
  • Ensure continuing compliance throughout software lifecycle

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International Professional & Industry Academy
10-12 Rivington Street
EC2A 3DU London

About IPI Academy

International Professional & Industry Academy (IPI) is an international leading professional training organisation based in London. Our training solutions provide a return on your investment with measurable results, and are delivered by experienced professionals and managed with exceptional care and...

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